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- Molybdenum_cofactor_deficiency abstract "Molybdenum cofactor deficiency is a rare human disease in which the absence of molybdenum cofactor leads to accumulation of toxic levels of sulphite and neurological damage. Usually this leads to death within months of birth, due to the lack of active sulfite oxidase. Furthermore, a mutational block in molybdenum cofactor biosynthesis causes absence of enyzme activity of xanthine dehydrogenase/oxidase and aldehyde oxidase.When caused by a mutation in the MOCS1 gene it is the type A variant. It can also be caused by a mutation in the MOCS2 gene or the GEPH gene. As of 2010, there had been approximately 132 reported cases.It should not be confused with molybdenum deficiency.".
- Molybdenum_cofactor_deficiency diseasesdb "29821".
- Molybdenum_cofactor_deficiency emedicineSubject "ped".
- Molybdenum_cofactor_deficiency emedicineTopic "2172".
- Molybdenum_cofactor_deficiency omim "252150".
- Molybdenum_cofactor_deficiency wikiPageID "20467061".
- Molybdenum_cofactor_deficiency wikiPageRevisionID "602259256".
- Molybdenum_cofactor_deficiency diseasesdb "29821".
- Molybdenum_cofactor_deficiency emedicinesubj "ped".
- Molybdenum_cofactor_deficiency emedicinetopic "2172".
- Molybdenum_cofactor_deficiency hasPhotoCollection Molybdenum_cofactor_deficiency.
- Molybdenum_cofactor_deficiency name "Molybdenum cofactor deficiency".
- Molybdenum_cofactor_deficiency omim "252150".
- Molybdenum_cofactor_deficiency subject Category:Vitamin,_coenzyme,_and_cofactor_metabolism_disorders.
- Molybdenum_cofactor_deficiency type Abstraction100002137.
- Molybdenum_cofactor_deficiency type Attribute100024264.
- Molybdenum_cofactor_deficiency type Condition113920835.
- Molybdenum_cofactor_deficiency type Disease114070360.
- Molybdenum_cofactor_deficiency type IllHealth114052046.
- Molybdenum_cofactor_deficiency type Illness114061805.
- Molybdenum_cofactor_deficiency type PathologicalState114051917.
- Molybdenum_cofactor_deficiency type PhysicalCondition114034177.
- Molybdenum_cofactor_deficiency type State100024720.
- Molybdenum_cofactor_deficiency type Disease.
- Molybdenum_cofactor_deficiency type AilmentCondition.
- Molybdenum_cofactor_deficiency type Situation.
- Molybdenum_cofactor_deficiency comment "Molybdenum cofactor deficiency is a rare human disease in which the absence of molybdenum cofactor leads to accumulation of toxic levels of sulphite and neurological damage. Usually this leads to death within months of birth, due to the lack of active sulfite oxidase. Furthermore, a mutational block in molybdenum cofactor biosynthesis causes absence of enyzme activity of xanthine dehydrogenase/oxidase and aldehyde oxidase.When caused by a mutation in the MOCS1 gene it is the type A variant.".
- Molybdenum_cofactor_deficiency label "Molybdenum cofactor deficiency".
- Molybdenum_cofactor_deficiency label "Molybdän-Cofaktor-Defizienz".
- Molybdenum_cofactor_deficiency label "Niedobór kofaktora molibdenowego".
- Molybdenum_cofactor_deficiency sameAs Molybdän-Cofaktor-Defizienz.
- Molybdenum_cofactor_deficiency sameAs Niedobór_kofaktora_molibdenowego.
- Molybdenum_cofactor_deficiency sameAs m.04zyjsg.
- Molybdenum_cofactor_deficiency sameAs Q1621463.
- Molybdenum_cofactor_deficiency sameAs Q1621463.
- Molybdenum_cofactor_deficiency sameAs 770.
- Molybdenum_cofactor_deficiency sameAs Molybdenum_cofactor_deficiency.
- Molybdenum_cofactor_deficiency wasDerivedFrom Molybdenum_cofactor_deficiency?oldid=602259256.
- Molybdenum_cofactor_deficiency isPrimaryTopicOf Molybdenum_cofactor_deficiency.
- Molybdenum_cofactor_deficiency name "Molybdenum cofactor deficiency".